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851305-26-5

851305-26-5 Structure

851305-26-5 Structure
IdentificationBack Directory
[Name]

(5Z)-5-[(5-phenylfuran-2-yl)methylidene]-3-prop-2-enyl-2-sulfanylidene-1,3-thiazolidin-4-one
[CAS]

851305-26-5
[Synonyms]

LJ 001 (LJ001
(Z)-3-Allyl-5-((5-phenylfuran-2-yl)methylene)-2-thioxothiazolidin-4-one
4-Thiazolidinone, 5-[(5-phenyl-2-furanyl)methylene]-3-(2-propen-1-yl)-2-thioxo-, (5Z)-
(5Z)-5-[(5-phenylfuran-2-yl)methylidene]-3-prop-2-enyl-2-sulfanylidene-1,3-thiazolidin-4-one
[Molecular Formula]

C17H13NO2S2
[MDL Number]

MFCD02120352
[MOL File]

851305-26-5.mol
[Molecular Weight]

327.42
Chemical PropertiesBack Directory
[Boiling point ]

477.3±55.0 °C(Predicted)
[density ]

1.37±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

-2.83±0.20(Predicted)
[color ]

Yellow to orange
Hazard InformationBack Directory
[Uses]

LJ001 is a broad-spectrum and orally active antiviral agent. LJ001 exerts antiviral activities by binding to viral membranes. LJ001 inhibits TGEV and PDCoV infection. LJ001 decreases TGEV N and PDCoV N-protein expression[1][2].
[in vivo]

LJ001 (20, 50 mg/kg; oral gavage or i.p.; daily for 7 days) shows no toxicity in mouse[2].

Animal Model:Female BALB/c mice[2]
Dosage:20, 50 mg/kg
Administration:Oral gavage or i.p.; daily for 7 days
Result:Revealed no abnormalities except a slight elevation in serum cholesterol levels in the treated vs. vehicle control group.
[References]

[1] Zhang Y, et al. Rhodanine derivative LJ001 inhibits TGEV and PDCoV replication in vitro. Virus Res. 2020 Nov;289:198167. DOI:10.1016/j.virusres.2020.198167
[2] Wolf MC, et al. A broad-spectrum antiviral targeting entry of enveloped viruses. Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3157-62. DOI:10.1073/pnas.0909587107
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